Ultrasmall Nanoparticles Diluted Chain Entanglement in Polymer Nanocomposites

被引:22
作者
Chai, Sheng-Chao [1 ]
Xu, Tian-Yang [1 ]
Cao, Xiao [2 ]
Wang, Gang [1 ]
Chen, Quan [2 ]
Li, Hao-Long [1 ]
机构
[1] Jilin Univ, Coll Chem, State Key Lab Supramol Struct & Mat, Changchun 130012, Jilin, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
Polymer nanocomposites; Ultrasmall nanoparticles; Chain entanglement; Polyoxometalates; POLYOXOMETALATE; HYBRID; REINFORCEMENT; DYNAMICS; VISCOSITY; DECREASE; BEHAVIOR; SHEET;
D O I
10.1007/s10118-019-2262-8
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Nanoparticle-polymer composites exhibit unusual mechanical properties and chain dynamics when the nanoparticle size is smaller than the entanglement mesh size of the matrix polymer chains, corresponding to the ultrasmall regime defined by de Gennes. However, the mechanism is still ambiguous due to the lack of suitable model systems. Here, we develop an ultrasmall nanoparticle system by using a bimodal grafting strategy to graft both short alkyl chains and long polystyrene chains onto the polyoxometalate molecular nanoparticles with a tunable repulsive potential between the nanoparticles, thus facilitating their uniform dispersion in polystyrene matrices. Linear viscoelasticity of the resultant nanocomposites changes with increasing the filler content, which shows a decrease in both plateau modulus and terminal relaxation time, indicative of a dilution effect of the nanoparticles. Namely, the entanglement network becomes sparser with increasing the filler content.
引用
收藏
页码:797 / 805
页数:9
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